Massive Hemoptysis in Loeys-Dietz Syndrome

被引:3
|
作者
Bennett, Christopher L. [1 ,2 ,3 ]
Aziz, Hamza [3 ]
Sparks, Elizabeth [3 ]
Shah, Trushil [4 ]
Yoder, Mark [4 ]
MacCarrick, Gretchen [3 ]
Dietz, Harry C. [2 ,3 ]
机构
[1] Univ N Carolina, Sch Med, Chapel Hill, NC USA
[2] Johns Hopkins Univ, Sch Med, Howard Hughes Med Inst, Baltimore, MD 21205 USA
[3] Johns Hopkins Univ, Sch Med, McKusick Nathans Inst Genet Med, Baltimore, MD 21205 USA
[4] Rush Univ, Med Ctr, Chicago, IL 60612 USA
关键词
Loeys-Dietz syndrome; hemoptysis; critical care; MUTATIONS; ANGIOGRAPHY;
D O I
10.1002/ajmg.a.37487
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe four unrelated individuals with Loeys-Dietz syndrome (LDS) who presented with massive hemoptysis of unknown etiology. LDS is an autosomal dominant connective-tissue disorder characterized by altered cardiovascular, craniofacial, and skeletal development that is attributed to mutations in the TGFBR1, TGFBR2, SMAD3, or TGFB2 genes. Massive hemoptysis (MH) is a rare and often fatal pulmonary medical emergency. This is the first report of MH in individuals with LDS and establishes it as part of the LDS spectrum. It compels providers to educate their LDS patients on MH, although much investigation needs to be done to determine etiology and appropriate treatment for this newly described LDS feature. (c) 2015 Wiley Periodicals, Inc.
引用
收藏
页码:725 / 727
页数:3
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